Evidence map›Paper›PMID 42650091›Full record

ArticleGenes2026

Epigenetic Regulation of Divergent Co-Expression Between Whole-Genome Duplication and Transposed Duplication Genes and Its Impact on Catechin Accumulation in

Shuaibin Lian, Huajin Feng, Haojie Hou, Liang Zhang, Youchao Tu, Ke Gong, Wei Zhang

Abstract read
In one paragraph

Article in Genes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Shuaibin LianCollege of Physics and Electronic Engineering, Xinyang Normal University, Xinyang 464000, China.
Huajin FengCollege of Physics and Electronic Engineering, Xinyang Normal University, Xinyang 464000, China.
Haojie HouCollege of Physics and Electronic Engineering, Xinyang Normal University, Xinyang 464000, China.
Liang ZhangCollege of Physics and Electronic Engineering, Xinyang Normal University, Xinyang 464000, China.
Youchao TuCollege of Physics and Electronic Engineering, Xinyang Normal University, Xinyang 464000, China.
Ke GongCollege of Physics and Electronic Engineering, Xinyang Normal University, Xinyang 464000, China.
Wei ZhangCollege of Life Sciences, Xinyang Normal University, Xinyang 464000, China.ORCID 0000-0002-8095-5178

Funding

Special Plan for Key Scientific Research Projects of Higher Education In-stitutions in Henan Province to Serve Industrial Development 25CY032
6 · The paper itself

Abstract

BACKGROUND/

objectivesWhole-genome duplication (WGD) and transposed duplication (TRD) are two principal evolutionary drivers of plant genome expansion, yet the molecular mechanisms underlying their divergent co-expression patterns remain poorly characterized.

methodsIn this study, based on the reference genome of tea plant (

resultsWGD gene pairs exhibited significantly higher co-expression rates (44.3%) than TRD pairs (33.0%), with gene length and sequence similarity jointly promoting co-expression. Chromatin accessibility and H3K27ac modification were each positively correlated with expression and co-expression; however, under equivalent chromatin accessibility conditions, TRD gene expression remained systematically attenuated, and this reduced expression state was significantly associated with elevated levels of CG, CHG, and CHH methylation, suggesting that these epigenetic marks may collectively participate in the transcriptional repression of TRD genes. Promoter-proximal SNPs exerted disproportionately deleterious effects on TRD co-expression, demonstrating that the combined effects of genetic variation and epigenetic modifications are associated with enhanced transcriptional divergence. Weighted gene co-expression network analysis (WGCNA) revealed that WGD modules showed significant associations with EC, GC, and EGC accumulation, whereas WRKY and bHLH transcription factors in the TRD MEblue module exhibited strong associations with EGCG and ECG.

conclusionsThis study systematically characterizes multi-omics association patterns related to duplicate gene co-expression divergence, providing insights into potential hierarchical regulation. It offers mechanistic clues for catechin metabolic regulation and provides candidate targets for metabolite-directed breeding.

Indexed as

Camellia sinensisCatechinEpigenesis, GeneticGene DuplicationGenome, PlantDNA MethylationGene Expression Regulation, PlantCatechincatechinschromatin accessibilityDNA methylationepigeneticstranscription factorstransposed duplicationwhole-genome duplication

Identifiers

PMID42650091
PMCPMC13512718

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.